An adjustable socket system includes a socket frame having a proximal area, a distal area opposite the proximal area, a first component arranged along a first side of the socket system, and a second component arranged along a second side of the socket system. The first component is connected to the second component. A tubular insert is arranged on an interior of at least the proximal area of the socket frame. The tubular insert forms an interior surface of the socket system. At least one tensioning element operatively connects the tubular insert to the first and/or second components. At least one tensioner is attached to the at least one tensioning element that selectively tensions the tensioning element to adjust a circumference of at least one area of the socket system.
A prosthetic system includes a prosthetic foot defining an upper surface and having a flexible configuration and a pump system attached to the prosthetic foot. The pump system includes a pump mechanism defining a fluid chamber having variable configuration and an actuating part. The actuating part is arranged to selectively engage with and separate a distance from the upper surface of the foot plate to move the pump mechanism between a first position in which a volume of the fluid chamber is zero or near-zero and a second position in which the volume of the fluid chamber is expanded relative to the first position. The volume of the fluid chamber increases when the actuating part moves away from the upper surface of the foot plate.
A cervical collar has a front component formed from a compressible foam material and defines a recess constituting part of a tracheal opening. The collar also has a height adjustment mechanism secured to the front component which forms a substantially rigid border about the tracheal opening, and a sternum pad formed from a compressible foam material. The height adjustment mechanism selectively connects the front component to the sternum pad at a permanently locked position among a plurality of predefined distances.
An adjustable prosthetic socket includes proximal and distal ends and an axis extending between the proximal and distal ends. A distal base is adapted to support a distal portion of a residual limb and is located at the distal end of the socket. First and second spines extend upward from the distal base that define at least part of a circumference of the socket about the axis. A proximal support is connected to the second spine and arranged to distribute pressure from the second spine over a portion of the residual limb. A tensioning system is operatively connected to the first and second spines and arranged to selectively adjust the circumference of the socket. The tensioning system includes a dial tensioner connected to the first spine.
A liner is arranged for use in prosthetic and orthopedic devices. The liner defines first and second end portions, and inner and outer surfaces. The liner includes an inner layer having a frictional component and forms at least part of the periphery of the inner liner surface. The inner layer defines a plurality of apertures. A porous element is in communication with the inner liner surface and is connected to the inner layer such that the apertures permit a transfer of air from the inner surface to the porous element. A base layer adjoins the porous element and extends between the first and second end portions of the liner.
An orthopedic device is provided for treating complications of the hip and has means for trochanter compression, pelvis support, lumbar compression, variously directed straps, and thigh support. The trochanter compression and an internal/external rotation strap provide pain relief through compression and skin protection, unloading of joints through compression and sealing, and unloading by load transfer. Means for adjustably dosing of straps enables pain management and ease of use.
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
7.
PROGRESSIVE FORCE STRAP ASSEMBLY FOR USE WITH AN ORTHOPEDIC DEVICE
A progressive strap assembly includes an elongate, inelastic body having first and second ends, and an elastic body having first and second ends, the first end of the elastic body anchored to the second end of the inelastic body. The elastic body is arranged to stretch a plurality of lengths and has a maximum stretchable length. A tension limiter is connected to the first and second ends of the elastic body and is arranged to inhibit a predetermined stretchable length of the elastic body short of the maximum stretchable length.
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
An adjustable socket system includes a socket frame having a proximal area, a distal area opposite the proximal area, a first component arranged along a first side of the socket system, and a second component arranged along a second side of the socket system. The first component is connected to the second component. A tubular insert is arranged on an interior of at least the proximal area of the socket frame. The tubular insert forms an interior surface of the socket system. At least one tensioning element operatively connects the tubular insert to the first and/or second components. At least one tensioner is attached to the at least one tensioning element that selectively tensions the tensioning element to adjust a circumference of at least one area of the socket system.
A suspension liner has a liner body portion, a textile material, and a plurality of seals formed along a length of the suspension liner toward a closed distal end and protruding circumferentially about a liner profile. Each seal has a same shape including a peak having a rounded profile and a width narrowing toward the peak and defines a sealing surface arranged to form a secure interface with an interior wall of the socket that retains the suspension liner within the prosthetic socket. The textile material is located intermediate interior and exterior surfaces of the suspension liner that formed of one or more silicone materials in the area of the seals and the textile material defines the exterior surface of the suspension liner proximal and distal to the seals.
An orthopedic device has various frame elements concealed by a sleeve defining pockets into which such frame elements are located. The orthopedic device includes a strap tightening assembly adapted to secure a plurality of straps simultaneously. The frame may include flexible edge features located along a periphery thereof.
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
11.
Method and device for ordering a custom orthopedic device
A method and device for digital measuring and ordering a custom orthopedic device includes an interactive method intended to assist clinicians select, measure and submit precise specifications for patients requiring custom orthopedic devices. The method includes a plurality of menus permitting the clinician to input specifications and submit orders electronically with the specifications and other data packaged together. The method and device include visualization indications to appropriately ensure image capture of a limb from various angles, including posterior, anterior, lateral and medial angles.
A61F 2/50 - Prostheses not implantable in the body
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
A spinal orthosis has an elongate and substantially rigid spinal frame having upper, middle and lower portions, and a lumbar assembly connected to the lower portion of the spinal frame. A strap assembly secures to an upper portion of the spinal frame and is adjustably secured to the lumbar assembly. An elastic strap has a first end secured to the spinal frame and a second end adjustably securing to the lumbar assembly.
In an embodiment, an orthopedic device in the form of a lumbar support includes first and second elongate belt members, an anatomically shaped plate, and a closure system connecting the belt members to the plate. The closure system is arranged to move the belt members relative to the plate, and connects to the belt members via a flexible belt attachment which removably secures to the belt members. The closure system includes tensioning elements corresponding to the belt members, and a pulley system connecting to the tensioning elements. The closure system is slidably mounted to the plate and arranged to the belt members relative to the plate between opposed linear directions. The plate has various contours which provide pressure distribution over a lumbar region of a back. Anatomically shaped and resiliently formed handles secure to the tensioning elements and the belt members.
A liner is arranged for use in prosthetic and orthopedic devices. The liner defines first and second end portions, and inner and outer surfaces. The liner includes an inner layer having a frictional component and forms at least part of the periphery of the inner liner surface. The inner layer defines a plurality of apertures. A porous element is in communication with the inner liner surface and is connected to the inner layer such that the apertures permit a transfer of air from the inner surface to the porous element. A base layer adjoins the porous element and extends between the first and second end portions of the liner.
An orthopedic device includes a textile panel having interior and exterior surfaces, and a first stabilizer assembly including a first tubular welt sewn or knitted within and extending from an exterior surface of the textile panel. A first cable is slidably extending through the tubular welt and a strap is connected to a first end of the cable extending from a first opening of the welt, and the strap is adjustably securable over the textile panel. The orthopedic device may include various portions of stretchability and features for receiving components for the orthopedic device.
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
A cervical collar has a chin support slidably connected to an inside surface of an anterior component adapted to secure against an anterior chin and neck of a user. A posterior component connects to the anterior component to circumferentially surround the user's neck. A height adjustment mechanism has spring locks securing the height adjustment mechanism against the anterior component. The cervical collar includes a footplate continuously extending from the height adjustment mechanism generally without a variation in thickness. The posterior component has side portions with a plurality of living hinges located proximate to elongate slots for straps connecting to the anterior component.
A seal component for a prosthetic liner comprises a base portion located at a distal portion of the seal component and anchored circumferentially to an exterior surface of the liner; a seal wall arranged to flexibly and movably extend relative to a body of the liner; at least two seal rings radially and outwardly extending from the seal wall; and an outwardly pitched portion at the distal end of the seal component and extends obliquely away from the base portion relative to the axis of the seal component, and an inwardly pitched portion at the proximal end of the seal component and extends obliquely toward the axis of the seal component, the at least two seal rings are located between the outwardly and inwardly pitched portions.
An orthopedic device has first and second struts connected to one another by a hinge system, and includes a dynamic control system and a counterforce system. The dynamic control system includes first and second dynamic components arranged on a first side of the orthopedic device to exert first and second dynamic forces according to a flexion angle of the hinge system. A counterforce system is located on a second side of the orthopedic device to counteract the first and second dynamic forces with at least one counterforce.
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
A vacuum assisted suspension system includes a prosthetic foot and a pump mechanism connected to the foot and fluidly couplable to a prosthetic socket. The pump mechanism includes an elongate pivoting member rotatable relative to the prosthetic foot about a joint and including a distal recess. A piston is connected to the foot and is movably received in the recess. A fluid chamber is defined between the piston and the interior of the recess. When no weight is placed on the foot a volume of the fluid chamber is zero or near-zero and when weight of a user is placed on the prosthetic foot the pivoting member rotates away from the piston and expands the volume of the fluid chamber to draw fluid into the fluid chamber from the prosthetic socket.
A versatile orthopedic device is arranged to convert between ligament and osteoarthritis treatment, and to accommodate a variety of leg anatomies. The orthopedic device is preferably configured as a double-upright brace indicating struts, frame component sections and associated hinges preferably intended to be along both medial and lateral sides of a wearer's leg. A strap kit with an unloading strap system may be added to the orthopedic device for conversion into an orthopedic device for osteoarthritis relief.
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
A progressive strap assembly includes an elongate, inelastic body having first and second ends, and an elastic body having first and second ends, the first end of the elastic body anchored to the second end of the inelastic body. The elastic body is arranged to stretch a plurality of lengths and has a maximum stretchable length. A tension limiter is connected to the first and second ends of the elastic body and is arranged to inhibit a predetermined stretchable length of the elastic body short of the maximum stretchable length.
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
An adjustable socket system includes a socket frame having a proximal area, a distal area opposite the proximal area, a first component arranged along a first side of the socket system, and a second component arranged along a second side of the socket system. The first component is connected to the second component. A tubular insert is arranged on an interior of at least the proximal area of the socket frame. The tubular insert forms an interior surface of the socket system. At least one tensioning element operatively connects the tubular insert to the first and/or second components. At least one tensioner is attached to the at least one tensioning element that selectively tensions the tensioning element to adjust a circumference of at least one area of the socket system.
An adjustable prosthetic socket includes proximal and distal ends and an axis extending between the proximal and distal ends. A distal base is adapted to support a distal portion of a residual limb and is located at the distal end of the socket. First and second spines extend upward from the distal base that define at least part of a circumference of the socket about the axis. A proximal support is connected to the second spine and arranged to distribute pressure from the second spine over a portion of the residual limb. A tensioning system is operatively connected to the first and second spines and arranged to selectively adjust the circumference of the socket. The tensioning system includes a dial tensioner connected to the first spine.
An orthopedic device has a rigid or semi-rigid frame element defining opposed first and second sides, and is adapted to extend about at least a portion of a limb. The device includes straps formed from a variety of segments having stretchable and substantially inelastic segments. The straps adjustably secure to the frame element, and stretch relative thereto. The device also includes a central strap pad arranged to connect two straps together such that a first strap of the two straps is movable relative to a second strap, and the first and second straps are maintained diagonal relative to one another.
A61F 5/00 - Orthopaedic methods or devices for non-surgical treatment of bones or jointsNursing devices
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
26.
Cervical collar having height and circumferential adjustment
A cervical collar has a front component formed from a compressible foam material and defines a recess constituting part of a tracheal opening. The collar also has a height adjustment mechanism secured to the front component which forms a substantially rigid border about the tracheal opening, and a sternum pad formed from a compressible foam material. The height adjustment mechanism selectively connects the front component to the sternum pad at a permanently locked position among a plurality of predefined distances.
A method and device for digital measuring and ordering a custom orthopedic device includes an interactive method intended to assist clinicians select, measure and submit precise specifications for patients requiring custom orthopedic devices. The method includes a plurality of menus permitting the clinician to input specifications and submit orders electronically with the specifications and other data packaged together. The method and device include visualization indications to appropriately ensure image capture of a limb from various angles, including posterior, anterior, lateral and medial angles.
A61F 2/50 - Prostheses not implantable in the body
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
41 - Education, entertainment, sporting and cultural services
42 - Scientific, technological and industrial services, research and design
Goods & Services
EDUCATIONAL SERVICES, namely, CONDUCTING CLASSES, SEMINARS, CONFERENCES, AND WORKSHOPS IN THE FIELDS OF MEDICAL PROCEDURES, PATIENT CARE DIAGNOSIS, PATIENT CARE CONSULTATION, OUTSOURCE MANUFACTURING, MARKETING, AND REVENUE CYCLE SUPPORT, AND REHABILITATION RELATED TO ORTHOTICS, PROSTHETICS, AND AMPUTATIONS PROVIDING A WEBSITE FEATURING NON-DOWNLOADABLE COMPUTER SOFTWARE FOR COORDINATING BUSINESS CONSULTATIONS, OUTSOURCE MANUFACTURING, EDUCATION, MARKETING, AND REVENUE CYCLE SUPPORT SERVICES RELATED TO PROSTHETICS, ORTHOTICS, REHABILITATION, AND AMPUTATIONS
An orthopedic device has an elongate, tubular body defining a patella opening located generally at a center portion of the tubular body. A patella buttress including a buttress pocket is located on the tubular body and about the patella opening. The buttress pocket has various stretchability characteristics relative to the tubular body. A buttress element is associated with the buttress pocket.
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
A suspension liner is provided for use as an interface between a residual limb and a prosthetic socket. The liner has an elongate, generally conical liner body formed from at least one material segment that is at least radially elastically extensible from a relaxed non-extended condition and including proximal and distal end areas, and a seal component connected to the liner body and having an exterior surface defining at least one exterior seal protruding from the exterior surface and extending radially outwardly from the seal component relative to a longitudinal axis of the liner body. The at least one interior seal is located along an interior surface of the seal component and defines at least one blade extending obliquely toward the liner body. A portion of the seal component carrying the interior seal extends freely and is movable relative to the liner body.
A support for an article has a body arranged for length adjustment along a length adjustment axis. A tensioning device is connected to the support and adjustment of the tensioning device shortens or lengthens a length of the support along the length adjustment axis. The body defines at least one opening overlapping at least part of the length adjustment axis such that length adjustment is governed by modification of the size of the at least one opening according to adjustment by the tensioning device.
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
A liner is arranged for use in prosthetic and orthopedic devices. The liner defines first and second end portions, and inner and outer surfaces. The liner includes an inner layer having a frictional component and forms at least part of the periphery of the inner liner surface. The inner layer defines a plurality of apertures. A porous element is in communication with the inner liner surface and is connected to the inner layer such that the apertures permit a transfer of air from the inner surface to the porous element. A base layer adjoins the porous element and extends between the first and second end portions of the liner.
A dynamic tension system connects to an orthopedic device having a frame and a hinge connected to the frame. The dynamic tension system includes a cable, an adjustment mechanism connected to the cable and arranged to incrementally wind or release the cable, and a tension control device connected to the adjustment mechanism and arranged to limit the adjustment mechanism from winding of the cable past a predetermined tension level.
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
34.
Prosthetic device, system and method for increasing vacuum attachment
A prosthetic system includes a prosthetic foot defining an upper surface and having a flexible configuration and a pump system attached to the prosthetic foot. The pump system includes a pump mechanism defining a fluid chamber having variable configuration and an actuating part. The actuating part is arranged to selectively engage with and separate a distance from the upper surface of the foot plate to move the pump mechanism between a first position in which a volume of the fluid chamber is zero or near-zero and a second position in which the volume of the fluid chamber is expanded relative to the first position. The volume of the fluid chamber increases when the actuating part moves away from the upper surface of the foot plate.
A spinal orthosis includes posterior panels arranged with a flat spinal curvature to create a reverse three-point pressure system to the spine. The reverse three-point pressure system relieves pressure on the posterior side of the vertebrae beneficial for certain indications. Various arrangements allow for securing the posterior panel to the spinal orthosis. The spinal orthosis includes a belt member length adjustment system including belt members having end portions reducible in length and a belt panel adapted to secure to the end portion of the belt member reduced in length to form at least in part a belt circumference of the spinal orthosis.
A prosthetic device includes first and second regions divided by a longitudinal line extending between the first and second ends of the device. The device has a continuously knit elasticized fabric layer including a first set of yarns located about a circumference of the device through the first and second regions. The fabric layer has different knit structures in the first and second regions to obtain different elasticity while sharing the first set of yarns so that the first region has a first elasticity, and the second region has a second elasticity greater than the elasticity of the first region. An elastomeric layer secures an interior surface of the fabric layer.
A61F 2/78 - Means for protecting prostheses or for attaching them to the body, e.g. bandages, harnesses, straps, or stockings for the limb stump
D04B 1/22 - Weft knitting processes for the production of fabrics or articles not dependent on the use of particular machinesFabrics or articles defined by such processes specially adapted for knitting goods of particular configuration
37.
Prosthetic device, system and method for increasing vacuum attachment
A prosthetic system includes a prosthetic valve having a valve body with a shaft defining a flow channel fluidly connectable to an interior of a socket. One or more ports in the valve body are in fluid communication with the flow channel and a membrane is positioned in the valve body. A release button associated with the membrane controls allow air flow into the socket via the one or more ports while air can flow out of the socket via the one or more ports independent of operation of the release button. A one-way valve is connected to the valve assembly that selectively permit air flow out of the socket. A valve insert is mountable on the socket and arranged to couple the valve body to the socket. The valve insert defines an opening configured to allow the shaft to extend through the valve insert and into the socket.
An orthopedic device has first and second elongate struts each having a strap coupling member, and a flexible strap securing to the first and second struts by the strap coupling members. The orthopedic device includes various embodiments of hinge assemblies including flexion and extension stops and locks for maintaining the hinge assembly in a fixed configuration. The orthopedic device has various embodiments of strap assemblies for securing components to cuff assemblies.
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
A vacuum assisted suspension system includes a prosthetic foot and a pump mechanism connected to the foot and fluidly couplable to a prosthetic socket. The pump mechanism includes an elongate pivoting member rotatable relative to the prosthetic foot about a joint and including a distal recess. A piston is connected to the foot and is movably received in the recess. A fluid chamber is defined between the piston and the interior of the recess. When no weight is placed on the foot a volume of the fluid chamber is zero or near-zero and when weight of a user is placed on the prosthetic foot the pivoting member rotates away from the piston and expands the volume of the fluid chamber to draw fluid into the fluid chamber from the prosthetic socket.
An orthopedic device has various frame elements concealed by a sleeve defining pockets into which such frame elements are located. The orthopedic device includes a strap tightening assembly adapted to secure a plurality of straps simultaneously. The frame may include flexible edge features located along a periphery thereof.
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
41.
Panel attachment and circumference adjustment systems for an orthopedic device
A spinal orthosis includes posterior panels arranged with a flat spinal curvature to create a reverse three-point pressure system to the spine. The reverse three-point pressure system relieves pressure on the posterior side of the vertebrae beneficial for certain indications. Various arrangements allow for securing the posterior panel to the spinal orthosis. The spinal orthosis includes a belt member length adjustment system including belt members having end portions reducible in length and a belt panel adapted to secure to the end portion of the belt member reduced in length to form at least in part a belt circumference of the spinal orthosis.
An adjustable prosthetic socket includes proximal and distal ends and an axis extending between the proximal and distal ends. A distal base is adapted to support a distal portion of a residual limb and is located at the distal end of the socket. First and second spines extend upward from the distal base that define at least part of a circumference of the socket about the axis. A proximal support is connected to the second spine and arranged to distribute pressure from the second spine over a portion of the residual limb. A tensioning system is operatively connected to the first and second spines and arranged to selectively adjust the circumference of the socket. The tensioning system includes a dial tensioner connected to the first spine.
An orthopedic device is provided for treating complications of the hip and has means for trochanter compression, pelvis support, lumbar compression, variously directed straps, and thigh support. The trochanter compression and an internal/external rotation strap provide pain relief through compression and skin protection, unloading of joints through compression and sealing, and unloading by load transfer. Means for adjustably dosing of straps enables pain management and ease of use.
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
An orthopedic device has a rigid or semi-rigid frame element defining opposed first and second sides, and is adapted to extend about at least a portion of a limb. The device includes straps formed from a variety of segments having stretchable and substantially inelastic segments. The straps adjustably secure to the frame element, and stretch relative thereto. The device also includes a central strap pad arranged to connect two straps together such that a first strap of the two straps is movable relative to a second strap, and the first and second straps are maintained diagonal relative to one another.
A61F 5/00 - Orthopaedic methods or devices for non-surgical treatment of bones or jointsNursing devices
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
A vacuum suspension system includes a pump mechanism operatively connectable to a prosthetic socket. The pump mechanism has a first member and a second member. An inflatable bladder is disposed between the first and second members. A fluid chamber is located between the first and second members and fluidly separate from the inflatable bladder. Inflation of the inflatable bladder mechanically separates the first and second parts to create a vacuum pressure in the fluid chamber.
F04B 45/04 - Pumps or pumping installations having flexible working members and specially adapted for elastic fluids having plate-like flexible members, e.g. diaphragms
An orthopedic device includes a hinge assembly, a frame having first and second frame components spaced apart from and connected to one another by the hinge assembly, a strap system extending between medial and lateral sides of the first frame component, and at least one tensioning element. The at least one tensioning element has a first end secured to the strap system and a second end coupled to the hinge assembly. Articulation of the hinge assembly pulls the strap system toward the frontal plane by the at least one tensioning element.
A61F 5/00 - Orthopaedic methods or devices for non-surgical treatment of bones or jointsNursing devices
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
An orthopedic device includes a textile panel having interior and exterior surfaces, and a first stabilizer assembly including a first tubular welt sewn or knitted within and extending from an exterior surface of the textile panel. A first cable is slidably extending through the tubular welt and a strap is connected to a first end of the cable extending from a first opening of the welt, and the strap is adjustably securable over the textile panel. The orthopedic device may include various portions of stretchability and features for receiving components for the orthopedic device.
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
A compliance assembly includes a compliance strap arranged to engage and extend around the exterior of an orthopedic device, and a compliance clasp attached to the compliance strap. The compliance clasp includes a base member, a door member, and a locking system. The door member is pivotally connected to the base member and is movable between an open position and a closed position in which the door member is rotated toward the base member and locks the compliance strap between the base and door members. The locking system is arranged to irreversibly lock the door member in the closed position.
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
A cervical collar including an anterior portion having a rigid or semi-rigid shell anterior main support piece. The anterior portion defines resilient or flexible edges formed along the periphery of the main support piece. The flexible edges form a three-dimensional anatomically configured proximal support portion defined along a proximal area of the anterior portion. The anterior main support piece defines a supporting spring portion centrally located along the proximal area of the anterior portion. The proximal support portion is formed around and encompasses the supporting spring portion.
A cervical collar has a chin support slidably connected to an inside surface of an anterior component adapted to secure against an anterior chin and neck of a user. A posterior component connects to the anterior component to circumferentially surround the user's neck. A height adjustment mechanism has spring locks securing the height adjustment mechanism against the anterior component. The cervical collar includes a footplate continuously extending from the height adjustment mechanism generally without a variation in thickness. The posterior component has side portions with a plurality of living hinges located proximate to elongate slots for straps connecting to the anterior component.
A liner is arranged for use in prosthetic and orthopedic devices. The liner defines first and second end portions, and inner and outer surfaces. The liner includes an inner layer having a frictional component and forms at least part of the periphery of the inner liner surface. The inner layer defines a plurality of apertures. A porous element is in communication with the inner liner surface and is connected to the inner layer such that the apertures permit a transfer of air from the inner surface to the porous element. A base layer adjoins the porous element and extends between the first and second end portions of the liner.
A thoracic lumbar sacral orthosis includes an upper body support for use with a torso orthosis. The upper body support has an anterior assembly including an anterior plate secured to the torso orthosis, a sternal assembly connected to the anterior plate, and a pectoral assembly connected to the sternal assembly. A posterior assembly is connected to the torso orthosis and is connected to the pectoral assembly by at least one strap. The sternal assembly has at least one pivot point arranged to pivot the sternal assembly relative to the anterior plate.
A prosthetic foot including a foot member and a heel member attached to a bottom surface of the foot member. A pump mechanism is located above the foot member and includes a housing and an elastomeric member at least in part defining a fluid chamber. The elastomeric member is operatively connected to the foot member such that when no weight is placed on the prosthetic foot the volume of the fluid chamber is zero or near-zero and upon heel strike the housing rotates relative to the foot member to expand the volume of the fluid chamber and draw fluid into the fluid chamber from a prosthetic socket in fluid communication with the pump mechanism.
A spinal orthosis has an elongate and substantially rigid spinal frame having upper, middle and lower portions, and a lumbar assembly connected to the lower portion of the spinal frame. A strap assembly secures to an upper portion of the spinal frame and is adjustably secured to the lumbar assembly. An elastic strap has a first end secured to the spinal frame and a second end adjustably securing to the lumbar assembly.
A prosthetic adapter including a lower connector, an upper connector rotatably coupled to the lower connector, and a locking mechanism for preventing the upper connector from rotating relative to the lower connector. The locking mechanism is arranged to generally automatically retain a locked position when the lower connector is rotated to an original, predetermined alignment. An activation member is connected to and arranged for operating the locking mechanism.
A suspension liner is provided for use as an interface between a residual limb and a prosthetic socket. The liner has an elongate, generally conical liner body formed from at least one material segment that is at least radially elastically extensible from a relaxed non-extended condition and including proximal and distal end areas, and a seal component connected to the liner body and having an exterior surface defining at least one exterior seal protruding from the exterior surface and extending radially outwardly from the seal component relative to a longitudinal axis of the liner body. The at least one interior seal is located along an interior surface of the seal component and defines at least one blade extending obliquely toward the liner body. A portion of the seal component carrying the interior seal extends freely and is movable relative to the liner body.
A strap tightener assembly has a base, a tightening device mounted on the base and movable relative thereto, and a strap assembly coupled to the tightening device. The tightening device provides incremental movement of the strap assembly relative to the base at a plurality of predefined settings. A cover extends over the strap assembly and connects to the base so that the base and the cover form a channel permitting movement of the strap assembly therethrough. The cover defines an elongate slot extending along a portion of a length of the cover, and the strap assembly has an indicator identifying the relative location of the strap assembly to the cover. A strap is securable to the strap assembly.
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
A44B 99/00 - Subject matter not provided for in other groups of this subclass
A strap attachment system includes a frame member having an opening, a strap, and a tab having a body and an attachment element defined by the body. The tab connects to the strap. A fastener element connects to the tab and is detachably and slidably mountable to the frame member by the opening.
A44B 11/28 - BucklesSimilar fasteners for interconnecting straps or the like, e.g. for safety belts with two or more separable parts with hooks engaging end-pieces on the strap
A44B 11/25 - BucklesSimilar fasteners for interconnecting straps or the like, e.g. for safety belts with two or more separable parts
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
A44B 11/00 - BucklesSimilar fasteners for interconnecting straps or the like, e.g. for safety belts
61.
Brim attachment with a seal element for a prosthetic socket
A brim attachment for a prosthetic socket includes a cuff section defining an upper portion of the brim attachment and is arranged to extend about and upwardly from a socket opening. The cuff section is configured to move between tensioned and relaxed positions, wherein the tensioned position the cuff section is arranged to fold away from the socket opening, wherein the relaxed position the cuff section is arranged to extend above the socket opening and generally concentric with an outer surface of the socket. An interface section defines a lower portion of the brim attachment and is arranged to extend along a surface of the socket. The brim attachment may include a seal element protruding toward a central axis of the socket.
A fastener member for mechanical affixation to a structure includes a base having first and second sides, a plurality of fastening elements integrally formed and extending from a first side of the base, and at least one affixation element extending from the second side of the base and arranged to mechanically affix to an attachment opening of a structure. A system includes a structure and a fastener member for mechanical affixation to the structure. A method includes affixing the fastener member to a structure.
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
A41D 13/05 - Professional, industrial or sporting protective garments, e.g. surgeons' gowns or garments protecting against blows or punches protecting only a particular body part
A44B 18/00 - Fasteners of the touch-and-close typeMaking such fasteners
In an embodiment, an orthopedic device in the form of a lumbar support includes first and second elongate belt members, an anatomically shaped plate, and a closure system connecting the belt members to the plate. The closure system is arranged to move the belt members relative to the plate, and connects to the belt members via a flexible belt attachment which removably secures to the belt members. The closure system includes tensioning elements corresponding to the belt members, and a pulley system connecting to the tensioning elements. The closure system is slidably mounted to the plate and arranged to the belt members relative to the plate between opposed linear directions. The plate has various contours which provide pressure distribution over a lumbar region of a back. Anatomically shaped and resiliently formed handles secure to the tensioning elements and the belt members.
A pin lock for a prosthetic device in a vacuum assisted suspension system includes a pin defining a longitudinally elongate bore and at least one passageway extending obliquely relative to the bore and communicating therewith at a proximal end of the pin. The pin lock also includes a locking mechanism having a receiving port arranged to receive the pin and a channel located at a distal end of the receiving port and adapted to communicate with the bore to exhaust air through the pin therefrom.
An orthopedic device has detachable components for treatment stages of an injury or surgical procedure. The orthopedic device is arranged as a protective functional support for regeneration of knee cartilage after surgical repair procedures, and includes a flexion control kit and a wrap-around liner sleeve.
A61F 5/00 - Orthopaedic methods or devices for non-surgical treatment of bones or jointsNursing devices
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
69.
Progressive strap assembly for use with an orthopedic device
A progressive strap assembly includes an elongate, inelastic body having first and second ends, and an elastic body having first and second ends, the first end of the elastic body anchored to the second end of the inelastic body. The elastic body is arranged to stretch a plurality of lengths and has a maximum stretchable length. A tension limiter is connected to the first and second ends of the elastic body and is arranged to inhibit a predetermined stretchable length of the elastic body short of the maximum stretchable length.
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
A vacuum suspension system includes a rigid socket defining a socket wall having exterior and interior surfaces. The socket defines an aperture extending between the exterior and interior surfaces, and has a closed distal end and an open proximal end with an interior cavity defined by the interior surface. A fluid regulator is provided at the aperture and operatively engages the fluid regulator. A pump system includes a pump and a covering for securing over the exterior surface of the socket and carrying the pump. The pump is configured for placement proximate to the fluid regulator and arranged for drawing air from the socket through the aperture. A chamber having a variable volume is formed by a space defined between the exterior surface and an inner surface of the covering proximate to the pump.
A coupling device for an orthopedic brace includes an anchoring member for securing to a frame and protruding therefrom, and a subshell arranged to connect to the frame by the anchoring member. The subshell has a locking element for selectively positioning the subshell on the frame at a plurality of locations. The subshell may include an end portion or contoured edge extending beyond a portion of the frame so as to flex relative to the frame.
A44B 11/00 - BucklesSimilar fasteners for interconnecting straps or the like, e.g. for safety belts
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
F16B 21/09 - Releasable fastening devices with a stud engaging a keyhole slot
A44B 11/25 - BucklesSimilar fasteners for interconnecting straps or the like, e.g. for safety belts with two or more separable parts
72.
Orthopedic device and method for securing the same
An orthopedic device has various frame elements concealed by a sleeve defining pockets into which such frame elements are located. The orthopedic device includes a strap tightening assembly adapted to secure a plurality of straps simultaneously. The frame may include flexible edge features located along a periphery thereof.
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
73.
Orthopedic device for treating complications of the hip
An orthopedic device is provided for treating complications of the hip and has means for trochanter compression, pelvis support, lumbar compression, variously directed straps, and thigh support. The trochanter compression and an internal/external rotation strap provide pain relief through compression and skin protection, unloading of joints through compression and sealing, and unloading by load transfer. Means for adjustably dosing of straps enables pain management and ease of use.
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
An orthopedic device has first and second struts connected to one another by a hinge system, and includes a dynamic control system and a counterforce system. The dynamic control system includes first and second dynamic components arranged on a first side of the orthopedic device to exert first and second dynamic forces according to a flexion angle of the hinge system. A counterforce system is located on a second side of the orthopedic device to counteract the first and second dynamic forces with at least one counterforce.
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
An alignment adapter for prosthetic sport feet, such as running feet, includes a male pyramid plate having a male pyramid, a female connector plate having a female connector, and a back plate. For use during alignment of a prosthetic running foot, the male pyramid plate is coupled to the back of a user's socket and the female connector plate and back plate are clamped about the foot. The male pyramid and female connector are coupled and adjusted relative to one another to achieve a desired alignment. The socket and foot are locked in an alignment fixture to maintain the alignment and the male pyramid, female connector, and back plates are removed. A laminated plate is coupled to the socket to maintain alignment during normal use.
A support for an article has a body arranged for length adjustment along a length adjustment axis. A tensioning device is connected to the support and adjustment of the tensioning device shortens or lengthens a length of the support along the length adjustment axis. The body defines at least one opening overlapping at least part of the length adjustment axis such that length adjustment is governed by modification of the size of the at least one opening according to adjustment by the tensioning device.
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
Prosthetic feet that provide for variable and adjustable stiffness are provided. A foot element can include a tongue portion defined or formed by a slot in the foot element that at least partially separates the tongue portion from a remainder of the foot element. The tongue portion can be operably connected to the remainder of the foot member to increase the stiffness of the foot member or operably disconnected from the remainder of the foot member to increase the flexibility of the foot member. The prosthetic foot further includes a mechanism for adjusting whether the tongue portion is operably connected or disconnected from the remainder of the foot member. The mechanism can be selectively actuated to adjust the stiffness of the foot element in dorsiflexion and/or plantarflexion and/or to adjust the degree to which the tongue portion is allowed to flex relative to the remainder of the foot member.
Prosthetic feet that provide for variable and adjustable stiffness are provided. A foot element can include a tongue portion defined or formed by a slot in the foot element that at least partially separates the tongue portion from a remainder of the foot element. The tongue portion can be operably connected to the remainder of the foot member to increase the stiffness of the foot member or operably disconnected from the remainder of the foot member to increase the flexibility of the foot member. The prosthetic foot further includes a mechanism for adjusting whether the tongue portion is operably connected or disconnected from the remainder of the foot member. The mechanism can be selectively actuated to adjust the stiffness of the foot element in dorsiflexion and/or plantarflexion and/or to adjust the degree to which the tongue portion is allowed to flex relative to the remainder of the foot member.
A thoracic lumbar sacral orthosis includes an upper body support for use with a torso orthosis. The upper body support has an anterior assembly including an anterior plate secured to the torso orthosis, a sternal assembly connected to the anterior plate, and a pectoral assembly connected to the sternal assembly. A posterior assembly is connected to the torso orthosis and is connected to the pectoral assembly by at least one strap. The sternal assembly has at least one pivot point arranged to pivot the sternal assembly relative to the anterior plate.
A vacuum assisted suspension system includes an elongate compression transfer element and a pump housing. The pump housing defines an enclosed space to receive a fluid. At least one wall of the housing and at least one movable wall define a fluid compartment and a non-fluid chamber. The at least one movable wall is connected to the compression transfer element. The compression transfer element causes the at least one movable wall of the fluid compartment to reciprocate in the fluid compartment to increase the volume of the fluid compartment in response to a compressive force on the compression transfer element and enables the at least one movable wall to decrease the volume of the fluid compartment in the absence of a compressive force.
An ankle module for a prosthetic foot can have an adapter portion pivotally coupled to a base portion. The base portion can be coupled to the prosthetic foot. The adapter portion can have a coupling member that removably couples the prosthetic foot to a prosthetic pylon or socket. The adapter portion can also have cylinders housing pistons slidably displaceable within the cylinders. An actuator is selectively actuatable to place the cylinders in fluid communication, allowing a fluid to flow between the cylinders as an angular position of the adapter portion is adjusted relative to the base portion, thereby adjusting the dorsi-plantar position between the adapter portion and the base portion of the ankle module. The actuator can be selectively actuatable to fluidly isolate the cylinders from each other so that the angular position of the adapter portion relative to the base portion remains substantially fixed.
Systems and apparatuses are provided comprising a prosthetic foot, a shock absorbing module and a coupling member for operably connecting the prosthetic foot to the shock absorbing module. The prosthetic foot can include an upper member connected to a lower member, wherein the upper member includes an upper attachment portion for attaching to the coupling member. The coupling member can include one or more holes for receiving an epoxy filling to secure the coupling member to the upper attachment portion of the prosthetic foot. The shock absorbing member can include a threaded portion that is mateable with an inner threaded section of the coupling member, thereby allowing height adjustability of the shock absorbing member.
A hinge for an orthopedic device includes a first part having a first end with a gear component, and a second part hingedly attached to the first part. The second part defines a cavity at a first end, and a worm is located within the cavity and engages the gear component. An adjustment element is adapted to regulate the worm relative to the gear component for articulating the first part relative to the second part.
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
An Achilles heel wedge has a front part, a back part, and a longitudinal axis extending in a longitudinal direction between the front part and the back part. A first wedge section defines a bottom surface and a top surface. The top surface of the first wedge section forms a convex portion curving along the longitudinal axis and extending between side portions of the first wedge section. The convex portion is positionable under the longitudinal arch of a user's foot during use. A second wedge section is removably attachable to the bottom surface of the first wedge section. The second wedge section defines substantially parallel top and bottom surfaces and a ramped edge at or near a front of the second wedge section. The ramped edge extends downwardly and forwardly relative to the first wedge section and the top surface of the second wedge section.
A43B 7/16 - Footwear with health or hygienic arrangements with foot-supporting parts with elevated heel parts inside
A43B 7/14 - Footwear with health or hygienic arrangements with foot-supporting parts
A43B 17/02 - Insoles for insertion, e.g. footbeds or inlays, for attachment to the shoe after the upper has been joined wedge-like or resilient
A43B 17/00 - Insoles for insertion, e.g. footbeds or inlays, for attachment to the shoe after the upper has been joined
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
Various features for improving the performance of prosthetic sport feet are provided. Prosthetic sport feet according to the present disclosure can be designed to improve performance in board sport activities, for example, surfing, windsurfing, kitesurfing, wakeboarding, skateboarding, snowboarding, skiing, and the like. A prosthetic board sports foot can have a wide profile and large area for contacting the board or ground to improve stability. The board sports foot can include a traction sole to reduce slippage on the board. The board sports foot can also include an attachment member for attaching the foot to a user's residual limb or another prosthetic component. The attachment member can include a tendon designed to allow for flexibility over an initial short range of movement. The tendon can be interchangeable, and tendons having various stiffnesses can be provided.
A versatile orthopedic device is arranged to convert between ligament and osteoarthritis treatment, and to accommodate a variety of leg anatomies. The orthopedic device is preferably configured as a double-upright brace indicating struts, frame component sections and associated hinges preferably intended to be along both medial and lateral sides of a wearer's leg. A strap kit with an unloading strap system may be added to the orthopedic device for conversion into an orthopedic device for osteoarthritis relief.
A61F 5/05 - Devices for stretching or reducing fractured limbsDevices for distractionsSplints for immobilising
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
90.
Tightening system with a tension control mechanism
A tightening system includes a housing and a spool situated within the housing. The spool is rotatable about an axis within the housing. An elongate tensioning element is rotatably linked to the spool and a tension control mechanism is operatively connected to the spool. The tension control mechanism is arranged to automatically move relative to the spool when tension in the tensioning element reaches a predetermined level, which, in turn, releases at least part of the tension in the tensioning element.
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
A prosthetic foot has a plate-like foot member with a core section substantially defined by one or more layers comprising a first material fiber, an upper section disposed above the core section, the upper section substantially defined by one or more layers comprising a second material fiber, and a lower section disposed below the core section, the lower section substantially defined by one or more layers comprising a third material fiber, where the upper, lower and core sections together define a total thickness of the plate-like elongate foot member. An idealized ratio of the cross sectional area of each section can be determined such that under an applied load provided to the hybrid layup, the ratio of maximum stress of a given section over the flexural strength of that given section is approximately equal for all sections of the hybrid layup. The hybrid layup arrangement can be configured to have a greater strength, but generally the same stiffness, as a similar foot member made of carbon fiber.
A vacuum suspension system includes a pump mechanism operatively connectable to a prosthetic socket. The pump mechanism has a first member and a second member. First and second fluid chambers are located between the first and second members. The second fluid chamber is fluidly separate from the first fluid chamber, and arranged for fluid communication with the socket. An increase in volume of the first fluid chamber mechanically expands the second fluid chamber, which, in turn, creates a vacuum pressure in the second fluid chamber.
F04B 45/04 - Pumps or pumping installations having flexible working members and specially adapted for elastic fluids having plate-like flexible members, e.g. diaphragms
An orthopedic device includes a posterior shell with ankle and foot receiving portions. The foot receiving portion defines a plantar shell portion and side shell portions extending along first and second sides of the plantar shell portion and forming an open-ended toe portion. A toe protector portion is removably attached to the posterior shell at the open-ended toe portion and arranged to protect the toes of the user. The toe protector portion extends between the side shell portions and longitudinally along a length of the side shell portions. At least one inflatable bladder is disposed in at least the ankle receiving portions and at least one pump assembly is in fluid communication with the at least one inflatable bladder.
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
Prosthetic feet and foot covers that provide a more natural appearance and improved performance are provided. A foot element for a prosthetic foot can extend from a heel end to a toe end and include a heel, arch, forefoot, and toe regions. The forefoot region can be wider than the arch and heel regions. The toe region can include a U- shaped cut out to define a big toe. Various features of the foot element can guide rollover of the foot through the big toe during use. A foot cover can be designed to receive a prosthetic foot including such a foot element. The foot cover can have a region of increased flexibility at a transition between the forefoot region and toe region. The foot cover can also have a padded area extending from the heel region across a lateral part of the arch region and forefoot region.
Prosthetic feet and foot covers that provide a more natural appearance and improved performance are provided. A foot element for a prosthetic foot can extend from a heel end to a toe end and include a heel, arch, forefoot, and toe regions. The forefoot region can be wider than the arch and heel regions. The toe region can include a U-shaped cut out to define a big toe. Various features of the foot element can guide rollover of the foot through the big toe during use. A foot cover can be designed to receive a prosthetic foot including such a foot element. The foot cover can have a region of increased flexibility at a transition between the forefoot region and toe region. The foot cover can also have a padded area extending from the heel region across a lateral part of the arch region and forefoot region.
An orthopedic device is arranged for dynamically treating the knee. The device includes a hinge assembly, a frame having an upper cuff and a lower cuff spaced apart from and connected by the hinge assembly, and a dynamic shell connected to the frame and extending along the first side of the brace. An adjustment system is connected to the dynamic shell and includes a tensioning element operatively engaging the shell and the hinge assembly. The adjustment system is arranged to increase and decrease tension in the tensioning element. The dynamic shell is arranged to be drawn toward the frontal plane as the orthopedic device goes from an extension orientation to a flexion orientation.
A61F 5/00 - Orthopaedic methods or devices for non-surgical treatment of bones or jointsNursing devices
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
A prosthetic knee for active users has a locking head generally parallel to a vertical axis of the prosthetic knee, a chassis, and a plurality of links connecting the locking head to the chassis. The knee includes a swing control mechanism having a flexion stop connected to the chassis and arranged to control the flexion angle of the knee. The flexion stop extends outwardly from the chassis and obliquely relative to the vertical axis. The knee has an audible feedback mechanism for providing the user with information about the location of the knee. The knee may also have a block lock forming a manually activated mechanism allowing load bearing in a flexed position.
A pad assembly comprises a padding defining first and second surfaces, and includes a first layer being resilient and accessible from the first surface and a second layer being resilient and underlying and secured to the first layer. The first and second removable sections are formed from at least one of the first and second layers and are arranged in a pattern and separated by edge clearances. Each of the first and second removable sections is tearable from the padding such that a residual portion of the removable section remains when at least one of the first and second removable sections is removed from the padding. The pad assembly may include a strap, and a substantially rigid or rigid shell connecting to the padding and strap.
A patellofemoral brace or support has a main substrate, a hinge located on at least one of the lateral and medial sides, and a support system coupled to the main substrate and the hinge. The support system has a compression element removably securable over the main substrate and a cable having a first end anchored to a pivoting element connected to the hinge and a second end anchored to the compression element. The cable engages the hinge such that articulation of the hinge from an extension position to a flexion position pulls the compression element toward the hinge to exert a generally medial force over the main substrate.
A61F 5/00 - Orthopaedic methods or devices for non-surgical treatment of bones or jointsNursing devices
A61F 5/01 - Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
